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  2. Sulfonic acid - Wikipedia

    en.wikipedia.org/wiki/Sulfonic_acid

    General structure of a sulfonic acid with the functional group indicated in blue. In organic chemistry, sulfonic acid (or sulphonic acid) refers to a member of the class of organosulfur compounds with the general formula R−S(=O) 2 −OH, where R is an organic alkyl or aryl group and the S(=O) 2 (OH) group a sulfonyl hydroxide. [1]

  3. Sodium hydroxide - Wikipedia

    en.wikipedia.org/wiki/Sodium_hydroxide

    2 Al + 2 NaOH + 2 H 2 O → 2 NaAlO 2 + 3 H 2 Sodium aluminate is an inorganic chemical that is used as an effective source of aluminium hydroxide for many industrial and technical applications. Pure sodium aluminate (anhydrous) is a white crystalline solid having a formula variously given as NaAlO 2 , Na 3 AlO 3 , Na[Al(OH) 4 ] , Na 2 O·Al 2 ...

  4. Conjugate (acid-base theory) - Wikipedia

    en.wikipedia.org/wiki/Conjugate_(acid-base_theory)

    An example of this case would be the splitting of hydrochloric acid HCl in water. Since HCl is a strong acid (it splits up to a large extent), its conjugate base (Cl −) will be weak. Therefore, in this system, most H + will be hydronium ions H 3 O + instead of attached to Cl − anions and the conjugate bases will be weaker than water molecules.

  5. Sodium sulfate - Wikipedia

    en.wikipedia.org/wiki/Sodium_sulfate

    The most important chemical sodium sulfate production is during hydrochloric acid production, either from sodium chloride (salt) and sulfuric acid, in the Mannheim process, or from sulfur dioxide in the Hargreaves process. [21] The resulting sodium sulfate from these processes is known as salt cake. Mannheim: 2 NaCl + H 2 SO 42 HCl + Na 2 SO 4

  6. Piranha solution - Wikipedia

    en.wikipedia.org/wiki/Piranha_solution

    Molecular models of the different molecules active in Piranha solution: peroxysulfuric acid (H 2 SO 5) and hydrogen peroxide (H 2 O 2). Piranha solution, also known as piranha etch, is a mixture of sulfuric acid (H 2 SO 4) and hydrogen peroxide (H 2 O 2). The resulting mixture is used to clean organic residues off substrates, for example ...

  7. Enthalpy change of solution - Wikipedia

    en.wikipedia.org/wiki/Enthalpy_change_of_solution

    Enthalpy change of solution in water at 25 °C for some selected compounds [2] Compound ΔH o in kJ/mol; hydrochloric acid: −74.84 ammonium nitrate +25.69 ammonia: −30.50 potassium hydroxide: −57.61 caesium hydroxide: −71.55 sodium chloride +3.87 potassium chlorate +41.38 acetic acid: −1.51 sodium hydroxide: −44.50

  8. Oxyacid - Wikipedia

    en.wikipedia.org/wiki/Oxyacid

    For example, carbon dioxide, CO 2, is the anhydride of carbonic acid, H 2 CO 3, and sulfur trioxide, SO 3, is the anhydride of sulfuric acid, H 2 SO 4. These anhydrides react quickly with water and form those oxyacids again. [4] Many organic acids, like carboxylic acids and phenols, are oxyacids. [3]

  9. Olin Raschig process - Wikipedia

    en.wikipedia.org/wiki/Olin_Raschig_process

    NaOCl + NH 3 → NH 2 Cl + NaOH. The monochloramine solution is then added to a 30-fold excess of ammonia at 130 °C and elevated pressure, causing a second reaction NH 2 Cl + NH 3 → N 2 H 4 + HCl. The hydrochloric acid and sodium hydroxide byproducts undergo a secondary reaction to release the byproducts of water and sodium chloride. The ...